I read no impact on VRUS into this news given that VRTX probably didn't want to cough up the amount of money that VRUS would have demanded and/or VRUS didn't want to partner with VRTX since VRUS can pretty much pick and choose who they want to partner with, if they want to partner at all.
However, I view this news as bearish for IDIX and INHX, since both have nukes that are further along than the ones VRTX licensed today.
I am just reading the PR now and Alios is Larry Blatt's company! He was at InterMune for quite some time. As an aside I believe Intermune had a poster a while back and Dan Welch had commented about a modest Polymerase program some time ago.
The $1.5B of total “biobucks” in the VRTX-Alios deal warrants an update of the table in #msg-40127105 with a new column for total biobucks (rather than just up-front cash). The Roche-VRUS deal for RG7128 also has to be added to the table.
This table does not purport to be exhaustive. Items are listed in descending order of biobucks; those shown in red resulted in an eventual buyout of the licensor by the licensee.
------$ Mln------ LicensorLicenseeProductPhaseClassUp-frontBiobucks DateiHub reference Alios VRTX ALS-2200 pc nuke 60 1,475 6/11 #msg-64166913 ANDS NVS ANA975 1 TLR7 20 570 2/05 #msg-6545305 IDIX NVS NM283 2 nuke 100‡ 555‡ 3/06 #msg-10407463 HGSI NVS Albuferon 2 ifn 45 553 6/06 #msg-11451787 VRTX JNJ Telaprevir 2 PI 165* 545* 6/06 #msg-11830934 ZGEN BMY Lambda 1 ifn 105 535 1/09 #msg-34768182 ITMN Roche ITMN-191 pc PI 60 530 10/06 #msg-14356850 LG Ltd GILD LB84451 2 CI 20 202 11/07 #msg-24337514 Genelabs GSK unnamed pc NN 13 188 5/06 #msg-11431616 VRTX Mitsbshi Telaprevir 3 PI 105† 170† 7/09 #msg-40126798 VRUS Roche RG7128 pc nuke 10 168 10/04 n/a Benitec PFE TT-033 pc RNAi n/a 145 1/08 #msg-25817504 Medivir JNJ TMC435 pc PI 10 n/a 11/04 n/a
*For rights in Europe, South America, Australia, and the Middle East. †For rights in Japan/Asia; monetization of amended 2004 agreement. ‡Includes $75M NVS paid for rights to NM283 and Telbivudine in 2003.
There was a median 4.54 log10 reduction in hepatitis C virus (HCV) RNA in people with genotype 1 chronic hepatitis C who were new to treatment (n=8) after seven days of dosing with 200 mg of ALS-2200 once daily. ALS-2200 was well-tolerated in this study, and no patients discontinued due to adverse events. Based on these data, Vertex plans to begin Phase 2 studies this year of 12-week all-oral regimens including ALS-2200 in people with genotype 1 hepatitis C, pending discussions with regulatory agencies…
Four of eight patients in this dose group achieved HCV RNA levels below the limit of quantification. Based on these data, Vertex expects to conduct a study to evaluate ALS-2200 in combination with INCIVEK (telaprevir), the company’s approved protease inhibitor for people with genotype 1 hepatitis C, and a study of ALS-2200 in combination with ribavirin.